Label: KANJO PAIN RELIEF GEL- menthol gel

  • NDC Code(s): 35192-039-02
  • Packager: CA-BOTANA INTERNATIONAL
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 20, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • OTC - ACTIVE INGREDIENT

    Menthol 5% Topical Analgesic

  • Other Safety Information

    Protect this product from excessive heat and direct sun

  • OTC - ASK DOCTOR

    Stop use and ask a doctor if redness is present.irritation develops. conditions worsens or symtoms persist more than 7 days. symtoms clear up and occur again within a few days

  • OTC - PURPOSE SECTION

    Uses: for temporary relief of minor aches and pains of muscles and joints associated with. simple aches. back aches. arthritis.strains.bruises.sprains.

  • Keep out of reach of children

    Keep out of reach of children

  • INACTIVE INGREDIENTS

    Aesculus hippocastanum (Horse Chestnut), Aloe barbadensis miller, Aloe barbadensis miller (Aloe Vera), Amonium Acrylcydimethyltaurate/VPCcopolymer, Arnica montana (Arnica), Bromelain, Butylene Glycol, Capsicum annum (Capsicum), Chamaemelum nobile (Chamomile), Ethyl alcohol, Eucalyptus globules (Eucaliptus) oil, FD&C Green # 3, Glucosamine Sulfate, Harpagophytum procumbens (Devil’s Claw), Melissa officinalis (Lemon Balm), Methyl Sulfonyl Methane (MSM), Polysorbate-60, Potassium Sorbate, Purified Water, Rosmarinus officinalis (Rosemary), Salix alba (Willow Bark), Edetic Acid, Tilia cordata (Linden), Xanthan Gum

  • Warnings

    Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

  • Dosage & Admnistration

    External topical analgesic Topical massage gel no more than 4 times daily

  • Indications & usage

    Apply generous amount of gel directly affected area massage into painful area until thoroughly absorbed into skin

  • Label

    Kanjo-Pain-relief-gel.jpg

  • INGREDIENTS AND APPEARANCE
    KANJO PAIN RELIEF GEL 
    menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:35192-039
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL6 g  in 120 g
    Inactive Ingredients
    Ingredient NameStrength
    CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    FD&C RED NO. 3 (UNII: PN2ZH5LOQY)  
    ARNICA MONTANA (UNII: O80TY208ZW)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SALIX ALBA BARK (UNII: 205MXS71H7)  
    HORSE CHESTNUT (UNII: 3C18L6RJAZ)  
    BROMELAINS (UNII: U182GP2CF3)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CAPSICUM (UNII: 00UK7646FG)  
    TILIA CORDATA FLOWER (UNII: CFN6G1F6YK)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    MELISSA OFFICINALIS (UNII: YF70189L0N)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    WATER (UNII: 059QF0KO0R)  
    ROSEMARY (UNII: IJ67X351P9)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    ALCOHOL (UNII: 3K9958V90M)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorMENTHOLImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:35192-039-02120 g in 1 TUBE; Type 0: Not a Combination Product08/31/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/31/2020
    Labeler - CA-BOTANA INTERNATIONAL (106276728)
    Establishment
    NameAddressID/FEIBusiness Operations
    CA-BOTANA INTERNATIONAL106276728manufacture(35192-039)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!